Implant having adjustable filament coils

ABSTRACT

Devices and methods for soft tissue reconstruction are provided. One exemplary embodiment of a device includes a body a suture filament extending through through-holes formed in the body. The suture is formed into an overhand knot having three collapsible openings with filament limbs extending from the knot. The limbs can be passed through the thru-holes of the body and selectively into the collapsible openings of the overhand knot to form coils extending to an opposite side of the body. For example, one limb can be passed through first and second collapsible openings to form two coils, while the other limb can be passed through the first and third collapsible openings to form two coils. The collapsible openings are collapsed around the limbs disposed in the openings, resulting in a secured overhand knot. Other configurations of knots, as well as devices and methods for use in tissue reconstruction, are also provided.

CROSS REFERENCE TO RELATED APPLICATIONS

The present application is a divisional of and claims priority to U.S.patent application Ser. No. 14/986,584, filed on Dec. 31, 2015, andentitled “Implant Having Adjustable Filament Coils,” which is acontinuation-in-part of and claims priority to U.S. patent Ser. No.13/793,514, filed on Mar. 11, 2013, and entitled “Implant HavingAdjustable Filament Coils,” and which issued as U.S. Pat. No. 9,974,643on May 22, 2018, each of which is hereby incorporated by reference inits entirety.

FIELD

The present disclosure relates to devices, systems, and methods forsecuring soft tissue to bone, and more particularly it relates tosecuring an ACL graft to a femur.

BACKGROUND

Joint injuries may commonly result in the complete or partial detachmentof ligaments, tendons, and soft tissues from bone. Tissue detachment mayoccur in many ways, e.g., as the result of an accident such as a fall,overexertion during a work related activity, during the course of anathletic event, or in any one of many other situations and/oractivities. These types of injuries are generally the result of excessstress or extraordinary forces being placed upon the tissues.

In the case of a partial detachment, commonly referred to under thegeneral term “sprain,” the injury frequently heals without medicalintervention, the patient rests, and care is taken not to expose theinjury to undue strenuous activities during the healing process. If,however, the ligament or tendon is completely detached from itsattachment site on an associated bone or bones, or if it is severed asthe result of a traumatic injury, surgical intervention may be necessaryto restore full function to the injured joint. A number of conventionalsurgical procedures exist for re-attaching such tendons and ligaments tobone.

One such procedure involves forming aligned femoral and tibial tunnelsin a knee to repair a damaged anterior cruciate ligament (“ACL”). In oneACL repair procedure, a ligament graft is associated with a surgicalimplant and secured to the femur. A common ACL femoral fixation meansincludes an elongate “button,” sometimes referred to as a corticalbutton. The cortical button is attached to a suture loop that is sizedto allow an adequate length of a soft tissue graft to lie within thefemoral tunnel while providing secure extra-cortical fixation.

Existing devices and methods can be limited because they do not alwaysprovide the desired strength. In some instances, one or more knots tiedto help maintain a location of the suture loop with respect to acortical button, and thus the graft associated therewith, can loosen orslip. Thus, even if a ligament graft is disposed at a desired locationduring a procedure, post-operatively the circumference of the loop canincrease, causing the graft to move away from the desired location.Further, it can be desirable to limit the number of knots used inconjunction with such devices, because of the potential for the knotsloosening and because the additional surface area knots can increase therisk of trauma. Some existing knot configurations used in conjunctionwith procedures of this nature can undesirably bind, which can preventthe knot from cinching down and leads to the knot having a higherprofile. Still further, existing devices and methods also lackadjustability in many instances. For example, in procedures in whichmultiple ligament grafts are associated with the cortical button, it canbe difficult to control placement of one ligament graft independently(i.e. without also moving the other ligament graft).

Accordingly, it is desirable to provide devices, systems, and methodsthat improve the strength and adjustability of surgical implants used inconjunction with ligament graft insertion, and to minimize the number ofknots associated with maintaining a location of the grafts once thegrafts are disposed at desired locations.

SUMMARY

Devices, systems, and methods are generally provided for performing ACLrepairs. In one exemplary embodiment, a surgical implant includes a bodyhaving a plurality of thru-holes and a suture filament extending throughthe body. The filament can be configured to form a knot and a pluralityof coils, with the knot being located on a top side of the body and aportion of each coil being disposed on both the top side of the body anda bottom side of the body as a result of the filament being disposedthrough at least two of the plurality of thru-holes of the body. Theknot can be a self-locking knot, with the self-locking knot defining acollapsible opening. The knot can have a portion of the suture filamentthat is intermediate its first terminal end and the plurality of coilsand is disposed on the top side of the body passed through thecollapsible opening from a first side of the opening. Further, the knotcan have a portion of the suture filament that is intermediate itssecond terminal end and the plurality of coils and disposed on the topside of the body passed through the collapsible opening from a second,opposite side of the opening. In some embodiments, the collapsibleopening can be configured to collapse and move toward the body whentension is applied to at least one of the first and second terminalends.

The plurality of coils can include a first coil and a second coil formedby a first portion of the filament extending between the self-lockingknot and the first terminal end, and a third coil and a fourth coilformed by a second portion of the filament extending between theself-locking knot and the second terminal end. In some embodiments thethru-holes of the body include two outer thru-holes and two innerthru-holes, with each outer thru-hole being located adjacent torespective opposed terminal ends of the body and the inner thru-holesbeing disposed between the outer thru-holes. In such embodiments, thefirst and third coils can pass through each of the outer thru-holes andthe second and fourth coils can pass through each of the innerthru-holes. Alternatively, in such embodiments, the first, second,third, and fourth coils can all pass through each of the innerthru-holes. At least one coil can be configured such that itscircumference can be changed by applying tension to at least one of thefirst and second terminal ends. In some embodiments the plurality ofcoils can be configured such that a circumference of one coil can beadjusted independent from adjusting a circumference of another coil.

The self-locking knot can include a Lark's Head knot. The Lark's Headknot can have certain modifications or additions to allow it to beself-locking, as described in greater detail herein. In some embodimentsthe implant can include a second suture filament extendinglongitudinally through the body. The second suture filament can passthrough each thru-hole of the plurality of thru-holes, and can be used,for example, as a shuttle to help guide the implant through a bonetunnel.

A sleeve can be included as part of the implant. A sleeve can bedisposed over a first portion of the suture filament that extendsbetween the self-locking knot and the first terminal end, and a sleevecan be disposed over a second portion of the suture filament thatextends between the self-locking knot and the second terminal end, witheach sleeve being located on the top side of the body. In someembodiments the sleeve disposed over the first portion and the sleevedisposed over the second portion can be the same sleeve, with a portionof that sleeve being disposed around the bottom side of the body.

Another exemplary embodiment of a surgical implant includes a bodyhaving a plurality of thru-holes formed therein and a suture filamentattached to the body such that the filament has a first terminal end, asecond terminal end, and a Lark's Head knot formed therein, all of whichare located on a top side of the body. The suture filament can bearranged with respect to the body such that a first portion of thefilament extending between the Lark's Head knot and the first terminalend passes through one thru-hole to a bottom side of the body andthrough a different thru-hole to the top side of the body to form afirst loop. Similarly, a second portion of the filament extendingbetween the Lark's Head knot and the second terminal end passes throughone thru-hole to the bottom side of the body and through a differentthru-hole to the top side of the body to form a second loop. Further,the first terminal end can pass through an opening defined by the Lark'sHead knot from a first side of the opening and the second terminal endcan pass through the same opening from a second, opposite side of theopening.

In some embodiments, additional loops can be formed from the suturefilament. For example, the suture filament can be arranged with respectto the body such that its first portion passes through one thru-hole tothe bottom side of the body and through a different thru-hole to the topside to form a third loop, while its second portion passes through onethru-hole to the bottom side of the body and through a differentthru-hole to the top side to form a fourth loop. In some embodiments thethru-holes of the body include two outer thru-holes and two innerthru-holes, with each outer thru-hole being located on an outer portionof the body and the inner thru-holes being disposed between the outerthru-holes. In such embodiments, the first and second portions of thesuture filament can pass through each of the outer thru-holes andthrough each of the inner thru-holes at least once. Alternatively, insuch embodiments, the first and second portions of the suture filamentcan pass through each of the inner thru-holes at least twice. A lengthof the filament's first portion and a length of the filament's secondportion can be adjustable. In some embodiments the implant can include asecond suture filament extending longitudinally through the body. Thesecond suture filament can pass through each thru-hole of the pluralityof thru-holes, and can be used, for example, as a shuttle to help guidethe implant through a bone tunnel.

One exemplary embodiment of a surgical method includes loading a graftonto one or more coils of a plurality of coils of an implant filamentthat is coupled to an implant body, pulling a leading end of a shuttlefilament that is disposed through the implant body through a bone tunneluntil the implant body is pulled out of the tunnel while at least aportion of the implant filament and the graft remain in the tunnel, andorienting the implant body so that its bottom side is facing the bonetunnel through which the implant body passed. Pulling the leading end ofthe shuttle filament also necessarily pulls the implant body, theimplant filament, and the graft through the tunnel. The resultingorientation of the implant's bottom side facing the tunnel is such thatthe plurality of coils are disposed substantially within the tunnel anda sliding knot first and second terminal ends of the implant filamentare located outside of the tunnel, adjacent to a top side of the implantbody.

In some embodiments, the step of orienting the implant body can beperformed by pulling a trailing end of the shuttle filament.Alternatively, the step of orienting the implant body can be performedby pulling both the leading and trailing ends of the shuttle filament.The method can further include selectively applying tension to at leastone of the first and second terminal ends to adjust a circumference ofone or more of the coils.

Yet another exemplary embodiment of a surgical implant includes a bodyhaving a plurality of thru-holes and a filament. The filament has anoverhand knot located on a top side of the body and a plurality of loopsthat extend from the overhand knot towards the body. The overhand knothas a first collapsible opening, a second collapsible opening, and athird collapsible opening. The loops can be a first filament loop, asecond filament loop, a third filament loop, and a fourth filament loop,with each filament loop passing through two thru-holes of the pluralityof thru-holes, and each filament loop having a distal end disposed on abottom side of the body. At least two tensioning limbs extend from theoverhand knot, in a direction opposite to a direction that the filamentloops extend from the overhand knot. A portion of filament of the firstfilament loop disposed on the top side of the body extends through thefirst collapsible opening, a portion of filament of the second filamentloop disposed on the top side of the body extends through the secondcollapsible opening, a portion of filament of the third filament loopdisposed on the top side of the body extends through the firstcollapsible opening, and a portion of filament of the fourth filamentloop disposed on the top side of the body extends through the thirdcollapsible opening. The first, second, and third collapsible openingsare collapsed around, and thus engaged with, the respective filamentsextending through the respective openings to form the overhand knot.

In some embodiments, the plurality of thru-holes can include two outerthru-holes and two inner thru-holes, with each outer thru-hole beinglocated adjacent to respective opposed terminal ends of the body and theinner thru-holes being disposed between the outer thru-holes. The firstand third filament loops can be disposed in each of the outer thru-holesand the second and fourth filament loops can be disposed in each of theinner thru-holes. Alternatively, the first, second, third, and fourthfilament loops each can be disposed in each of the inner thru-holes.

At least one of the at least two tensioning limbs can be configured toadjust a circumference of at least one of the first, second, third, andfourth filament loops when tension is applied to the limb(s). Further,the first collapsible opening can have a central location such that thesecond collapsible opening is located on one side of the firstcollapsible opening and the third collapsible opening is located on asecond, approximately opposite side of the first collapsible opening.Moreover, the first, second, third, and fourth filament loops of therecited embodiments can hold a combined average maximum load of at leastabout 765 N.

In a further exemplary embodiment a surgical implant includes a bodyhaving a plurality of thru-holes formed therein and a suture filamentextending through the body. The suture filament is configured to form anoverhand knot located on a top side of the body with the knot having afirst collapsible opening, a second collapsible opening, and a thirdcollapsible opening. A first coil is formed by extending a first suturelimb from the overhand knot, through a through hole of the plurality ofthru-holes formed in the body to a bottom side of the body, then throughanother through hole formed in the body, and then through the firstcollapsible opening of the overhand knot. A second coil is similarlyformed by extending a second suture limb from the overhand knot, througha through hole of the plurality of thru-holes formed in the body to thebottom side of the body, then through another through hole formed in thebody, and then through one of the first, second, and third collapsibleopenings of the overhand knot. A third coil is formed by extending thefirst suture limb, which has already passed through the firstcollapsible opening, through a through hole of the plurality ofthru-holes formed in the body to the bottom side of the body, thenthrough another through hole formed in the body, and then through thesecond collapsible opening of the overhand knot. A portion of the firstsuture limb that extends through the second collapsible opening forms afirst tensioning limb. A fourth coil is likewise formed by extending thesecond suture limb, which has already passed through one of the first,second, and third collapsible openings, through a through hole of theplurality of thru-holes formed in the body to the bottom side of thebody, then through another through hole formed in the body, and thenthrough either the third opening of the overhand knot if the secondsuture limb did not previously extend through the third opening, or oneof the first and second collapsible openings of the overhand knot if thesecond suture limb did extend through the third opening. A portion ofthe second suture limb that extends through either the third collapsibleopening, or one of the first and second collapsible openings, forms asecond tensioning limb. The first, second, and third collapsibleopenings are collapsed around, and thus engaged with, the respectivefirst and second suture limbs extending through the respective openingsto form the overhand knot.

In some embodiments the plurality of thru-holes can include two outerthru-holes and two inner thru-holes, with each outer thru-hole beinglocated adjacent to respective opposed terminal ends of the body and theinner thru-holes being disposed between the outer thru-holes. The firstand third coils can be disposed in each of the outer thru-holes and thesecond and fourth coils can be disposed in each of the inner thru-holes.Alternatively, the first, second, third, and fourth coils each can bedisposed in each of the inner thru-holes.

At least one of the first and second tensioning limbs can be configuredto adjust a circumference of at least one of the respective first andthird coils and second and fourth coils when tension is applied to thelimb(s). Further, the first collapsible opening can have a centrallocation such that the second collapsible opening is located on one sideof the first collapsible opening and the third collapsible opening islocated on a second, approximately opposite side of the firstcollapsible opening. Moreover, the first, second, third, and fourthcoils of the recited embodiments can hold a combined average maximumload of at least about 765 N.

In another exemplary method of configuring a surgical implant, themethod can include manipulating a filament to form a knot having a firstcollapsible opening, a second collapsible opening, and a thirdcollapsible opening, the filament having first and second limbsextending from the knot. The filament is coupled to the implant body bypassing the first and second limbs from a first side of an implant bodyto a second side of the implant body, and then from the second side tothe first side of the implant body. Back on the first side, the firstlimb is passed through the first collapsible opening, and the secondlimb is passed through one of the first, second, and third collapsibleopenings. The first and second limbs are again passed from the firstside to the second side of the implant body, and from the second side tothe first side. The first limb is then passed through one of the secondand third collapsible openings, while the second limb is passed througha different collapsible opening of the first, second, and thirdcollapsible openings from which it was passed previously. Morespecifically, the different collapsible opening is the collapsibleopening through which neither the first limb nor the second limb hasbeen passed if neither the first limb nor the second limb has beenpassed through one of the first, second, and third collapsible openingsduring the three previously recited passes by the first and second limbsthrough the first, second, and third collapsible openings. The methodfurther includes collapsing the first, second, and third collapsibleopenings to engage the first and second limbs passed through theopenings with a portion of the filament that forms each of thecollapsible openings.

In some embodiments the first collapsible opening can have a centrallocation such that the second collapsible opening is located on one sideof the first collapsible opening and the third collapsible opening islocated on a second, approximately opposite side of the firstcollapsible opening. The method can further include applying tension toa portion of at least one of the first and second limbs extending fromthe knot after the first, second, and third openings are collapsed toadjust a circumference of at least one of the respective first, second,third, and fourth coils.

The method can be such that a first time the first limb is passed fromthe first side of the implant body to the second side of the implantbody, the first limb can be passed through one opening of a plurality ofopenings formed in the implant body, and a first time the first limb ispassed from the second side of the implant body to the first side of theimplant body, the first limb can be passed through another opening ofthe plurality of openings formed in the implant body, thereby forming afirst coil. Further, a first time the second limb is passed from thefirst side of the implant body to the second side of the implant body,the second limb can be passed through one opening of the plurality ofopenings formed in the implant body, and a first time the second limb ispassed from the second side of the implant body to the first side of theimplant body, the second limb can be passed through another opening ofthe plurality of openings formed in the implant body, thereby forming asecond coil. In such embodiments, a second time the first limb is passedfrom the first side of the implant body to the second side of theimplant body, the first limb can be passed through one opening of theplurality of openings formed in the implant body, and a second time thefirst limb is passed from the second side of the implant body to thefirst side of the implant body, the first limb can be passed throughanother opening of the plurality of openings formed in the implant body,thereby forming a third coil. A second time the second limb is passedfrom the first side of the implant body to the second side of theimplant body, the second limb can be passed through one opening of theplurality of openings formed in the implant body, and a second time thesecond limb is passed from the second side of the implant body to thefirst side of the implant body, the second limb can be passed throughanother opening of the plurality of openings formed in the implant body,thereby forming a fourth coil.

The plurality of openings formed in the implant body can include twoouter openings and two inner openings, with each outer opening beinglocated adjacent to respective opposed terminal ends of the implant bodyand the inner openings being disposed between the outer openings. Aportion of the first and second limbs that respectively form the firstand second coils can be disposed in each of the inner thru-holes and aportion of the first and second limbs that respectively form the thirdand fourth coils can be disposed in each of the outer thru-holes.Alternatively, the plurality of openings can include two openings, and aportion of the first and second limbs that respectively form the firstand third coils and the second and fourth coils can be disposed in eachof the two openings.

In some embodiments, a first time the first limb is passed from thefirst side of the implant body to the second side of the implant body,the first limb can be passed around a first lateral side of the implantbody, and a first time the first limb is passed from the second side ofthe implant body to the first side of the implant body, the first limbcan be passed around a second lateral side of the implant body that isopposed to the first lateral side, thereby forming a first coil.Likewise, a first time the second limb is passed from the first side ofthe implant body to the second side of the implant body, the second limbcan be passed around one of the first and second lateral sides of theimplant body, and a first time the second limb is passed from the secondside of the implant body to the first side of the implant body, thesecond limb can be passed around the other of the first and secondlateral sides of the implant body, thereby forming a second coil. Insuch embodiments, a second time the first limb is passed from the firstside of the implant body to the second side of the implant body, thefirst limb can be passed around one of the first and second lateralsides of the implant body, and a second time the first limb is passedfrom the second side of the implant body to the first side of theimplant body, the first limb can be passed around the other of the firstand second lateral sides of the implant body, thereby forming a thirdcoil. Likewise, in such embodiments, a second time the second limb ispassed from the first side of the implant body to the second side of theimplant body, the second limb can be passed around one of the first andsecond lateral sides of the implant body, and a second time the secondlimb is passed from the second side of the implant body to the firstside of the implant body, the second limb can be passed around the otherof the first and second lateral sides of the implant body, therebyforming a fourth coil.

Unless otherwise specified, the steps of the methods provided for in thepresent disclosure can be performed in any order.

BRIEF DESCRIPTION OF DRAWINGS

This invention will be more fully understood from the following detaileddescription taken in conjunction with the accompanying drawings, inwhich:

FIG. 1A is a schematic view of components of one exemplary embodiment ofa surgical implant, including a cortical button and a suture filamenthaving a Lark's Head knot formed therein;

FIG. 1B is a perspective side view of one exemplary embodiment of asurgical implant formed using the cortical button and suture filament ofFIG. 1A;

FIG. 2A is a top perspective view of the cortical button of FIG. 1A;

FIG. 2B is an end elevational view of the cortical button of FIG. 2A;

FIG. 2C is a side elevational view of the cortical button of FIG. 2A;

FIGS. 3A-3E are sequential views illustrating one exemplary embodimentfor forming the Lark's Head knot of FIG. 1A;

FIG. 4 is a schematic side cross-sectional view of one exemplaryembodiment of a surgical implant;

FIG. 5 is a schematic side cross-sectional view of another exemplaryembodiment of a surgical implant;

FIGS. 6A-6B are sequential views of yet another exemplary embodiment ofa surgical implant, the implant having grafts associated therewith,illustrating selective movement of the grafts;

FIGS. 7A-7E are sequential views illustrating one exemplary embodimentof coupling a suture to a cortical button to form a surgical implant;

FIG. 8A-D are sequential views illustrating one exemplary embodiment ofcoupling a suture to an implant;

FIG. 9A is a schematic side cross-sectional view of another exemplaryembodiment of a surgical implant;

FIG. 9B is a side perspective view of the surgical implant of FIG. 9Awith a knot of the implant in a collapsed configuration;

FIG. 10 is a schematic side cross-sectional view of another exemplaryembodiment of a surgical implant;

FIGS. 11A-11H are sequential views illustrating another exemplaryembodiment of coupling a suture to a cortical button to form a surgicalimplant, and associating a graft therewith;

FIG. 12 is a side perspective view of another exemplary embodiment of asurgical implant;

FIG. 13 is a side perspective view of one exemplary embodiment of asurgical implant associated with a shuttle filament;

FIG. 14A is a schematic side cross-sectional view of another exemplaryembodiment of a surgical implant associated with a shuttle filament;

FIG. 14B is a top view of a body of the surgical implant of FIG. 14A;

FIG. 15A is a schematic side cross-sectional view of still anotherexemplary embodiment of a surgical implant associated with a shuttlefilament;

FIG. 15B is a top view of a body of the surgical implant of FIG. 15A;

FIG. 16A is a schematic view of a portion of one exemplary embodimentfor implanting a graft in a bone tunnel using a surgical implant havinga shuttle filament associated therewith;

FIG. 16B is a schematic view of the surgical implant of FIG. 15A for usein the exemplary embodiment for implanting a graft in a bone tunnel ofFIGS. 16A and 16D-H;

FIG. 16C is a schematic view of the surgical implant of FIG. 14A for usein the exemplary embodiment for implanting a graft in a bone tunnel ofFIGS. 16A and 16D-H;

FIGS. 16D-G are schematic, sequential views illustrating the remainderof the exemplary embodiment for implanting a graft in a bone tunnel ofFIG. 16A; and

FIG. 16H is a schematic view of a portion of another exemplaryembodiment for implanting a graft in a bone tunnel using a surgicalimplant having two, independently collapsible coils.

DETAILED DESCRIPTION

Certain exemplary embodiments will now be described to provide anoverall understanding of the principles of the structure, function,manufacture, and use of the devices and methods disclosed herein. One ormore examples of these embodiments are illustrated in the accompanyingdrawings. Those skilled in the art will understand that the devices andmethods specifically described herein and illustrated in theaccompanying drawings are non-limiting exemplary embodiments and thatthe scope of the present invention is defined solely by the claims. Thefeatures illustrated or described in connection with one exemplaryembodiment may be combined with the features of other embodiments. Suchmodifications and variations are intended to be included within thescope of the present invention. Further, in the present disclosure,like-numbered components of the embodiments generally have similarfeatures. Additionally, to the extent that linear or circular dimensionsare used in the description of the disclosed systems, devices, andmethods, such dimensions are not intended to limit the types of shapesthat can be used in conjunction with such systems, devices, and methods.A person skilled in the art will recognize that an equivalent to suchlinear and circular dimensions can easily be determined for anygeometric shape. Sizes and shapes of the systems and devices, and thecomponents thereof, can depend at least on the anatomy of the subject inwhich the systems and devices will be used, the size and shape ofcomponents with which the systems and devices will be used, and themethods and procedures in which the systems and devices will be used.

The figures provided herein are not necessarily to scale. Further, tothe extent arrows are used to describe a direction a component can betensioned or pulled, these arrows are illustrative and in no way limitthe direction the respective component can be tensioned or pulled. Aperson skilled in the art will recognize other ways and directions forcreating the desired tension or movement. Likewise, while in someembodiments movement of one component is described with respect toanother, a person skilled in the art will recognize that other movementsare possible. By way of non-limiting example, in embodiments in which asliding knot is used to help define a collapsible loop, a person skilledin the art will recognize that different knot configurations can changewhether moving the knot in one direction will cause a size of an openingdefined by the knot will increase or decrease. Additionally, a number ofterms may be used throughout the disclosure interchangeably but will beunderstood by a person skilled in the art. By way of non-limitingexample, the terms “suture” and “filament” may be used interchangeably.

The present disclosure generally relates to a surgical implant for usein surgical procedures such as ACL repairs. The implant can include abody having thru-holes formed therein and a suture filament associatedtherewith. An exemplary embodiment of a body 10 and a suture filament 50illustrated separately is shown in FIG. 1A, while an exemplaryembodiment of the two components coupled together to form an implant 100is shown in FIG. 1B. The suture filament 50 can form a self-locking knot52, illustrated as including a Lark's Head knot in FIG. 1A, and firstand second tails 54, 55 extending therefrom can be passed throughthru-holes 24 formed in the body 10 to associate the two components. Asdescribed below, the self-locking knot 52 is actually a Lark's Head knotmodified to make it self-locking.

While the particulars of the formation of the construct illustrated inFIG. 1B are discussed in greater detail below, as shown the self-lockingknot 52 can be formed on a first, top side 10 a of the body 10 and aplurality of coils 60 formed from the first and second tails 54, 55extending from the self-locking knot 52 can be disposed on a second,bottom side 10 b of the body 10. First and second terminal ends 54 t, 55t of the first and second tails 54, 55 can be passed through acollapsible opening 56 (FIGS. 4 and 5) of the self-locking knot 52before the knot 52 is collapsed, with the second terminal end 55 tpassing through the collapsible opening 56 from a first side 56 a of theopening 56, and the first terminal end 54 t passing through thecollapsible opening 56 from a second, opposite side 56 b of the opening56. As shown, the terminal ends 54 t, 55 t can extend proximally fromthe self-locking knot 52, and the collapsible opening 56 can beconfigured to collapse and move toward the body 10 when tension isapplied to at least one of the terminal ends 54 t, 55 t. Applyingtension to the terminal ends 54 t, 55 t can also selectively adjust acircumference of one or more of the coils 60 without adjusting acircumference of all of the coils 60. Optionally, a sleeve 58 can beassociated with one or both of the tail portions extending between theself-locking knot 52 and the first and second terminal ends 54 t, 55 t.The sleeve 58 can help prevent the tails 54, 55 from being cut too closeto the knot 52 after a desired implant location is achieved.

A body 10 for use as a part of a surgical implant to fixate a ligamentgraft in bone is illustrated in FIGS. 2A-2C. The body 10 can have asomewhat rectangular, elongate shape with curved leading and trailingterminal ends 16, 18. A plurality of thru-holes 24 can extend from afirst, top surface 20 and through a second, bottom surface 22. In theillustrated embodiment there are two outer thru-holes 24 a, 24 ddisposed, respectively, adjacent to leading and trailing terminal ends16, 18, and two inner thru-holes 24 b, 24 c disposed between the twoouter holes 24 a, 24 d. As shown, the outer and inner thru-holes 24 a,24 d and 24 b, 24 c have diameters that are substantially the same, anda space separating adjacent thru-holes 24 is substantially the same foreach adjacent pair. A width W of the body 10 is defined by the distancebetween the two elongate sidewalls 12, 14, as shown in FIG. 2B, a lengthL of the body 10 is defined by the distance between central portions 16c, 18 c of the end walls of the leading and trailing terminal ends 16,18, as shown in FIG. 2C, and a thickness T of the body 10 is defined bythe distance between the top and bottom surfaces 20, 22, as shown inFIGS. 2B and 2C. The body 10 can generally be referred to as a corticalbutton, among other known terms.

A person skilled in the art will recognize that the body 10 describedherein is merely one example of a body that can be used in conjunctionwith the teachings provided herein. A body configured to be associatedwith a suture filament of the type described herein can have a varietyof different shapes, sizes, and features, and can be made of a varietyof different materials, depending, at least in part, on the othercomponents with which it is used, such as the suture filament and theligament graft, and the type of procedure in which it is used. Thus,while in the present embodiment the body 10 is somewhat rectangularhaving curved ends, in other embodiments the body can be substantiallytubular, among other shapes.

In one exemplary embodiment of the substantially rectangular button, thelength L of the body is in the range of about 5 millimeters to about 30millimeters, the width W is in the range of about 1 millimeter to about10 millimeters, and the thickness T is in the range of about 0.25millimeters to about 3 millimeters. In one exemplary embodiment, thelength L can be about 12 millimeters, the width W can be about 4millimeters, and the thickness T can be about 1.5 millimeters. Diametersof the thru-holes 24 can be in the range of about 0.5 millimeters toabout 5 millimeters, and in one exemplary embodiment each can be about 2millimeters. Although in the illustrated embodiment each of thethru-holes 24 a, 24 b, 24 c, 24 d has a substantially similar diameter,in other embodiments some of the thru-holes can have differentdiameters. Additionally, any number of thru-holes can be formed in thebody 10, including as few as two.

In exemplary embodiments the body 10 can be made from a stainless steelor titanium, but any number of polymers, metals, or other biocompatiblematerials in general can be used to form the body. Some non-limitingexamples of biocompatible materials suitable for forming the bodyinclude a polyether ether ketone (PEEK), bioabsorbable elastomers,copolymers such as polylactic acid-polyglycolic acid (PLA-PGA), andbioabsorbable polymers such as polylactic acid. The implant can also beformed of absorbable and non-absorbable materials. Other exemplaryembodiments of a body or cortical button that can be used in conjunctionwith the teachings herein are described at least in U.S. Pat. No.5,306,301 of Graf et al., the content of which is incorporated byreference herein in its entirety.

Steps for configuring the suture filament 50 for use as a part of thesurgical implant 100 to fixate a ligament graft in bone are illustratedin FIGS. 3A-3E. As shown in FIG. 3A, the filament can be foldedsubstantially in half at an approximate midpoint 50 m of the filament50, forming a first filament limb 54 and a second filament limb 55having first and second terminal ends 54 t and 55 t, respectively. Acentral portion 50 c of the filament 50, which includes the midpoint 50m, can be folded toward the first and second limbs 54, 55, as shown inFIG. 3B, and be brought proximate to the first and second limbs 54, 55.This results in the formation of a first secondary loop 57 and a secondsecondary loop 59, as shown in FIG. 3C. A size of the secondary loops57, 59, and a length of the limbs 54, 55 extending therefrom, can beadjusted as desired.

As shown in FIG. 3D, a portion 54 p, 55 p of the first and second limbs54, 55 that are part of the secondary loops 57, 59 can be grasped andpulled upward (as shown, “out of the page”). This results in theconfiguration illustrated in FIG. 3E, a filament having a Lark Head'sknot 52 formed therein with first and second filament limbs 54, 55having terminal ends 54 t, 55 t extending therefrom. The Lark's Headknot 52 defines a collapsible opening 56, a size of which can bedecreased by applying a force in an approximate direction A to one orboth of the limbs 54, 55 extending from the knot 52, or by applying aforce in an approximate direction B to the opening 56. Likewise, a sizeof the opening 56 can be increased by grasping near the midpoint 50 m ofthe filament 50 to hold the portion where the fold is formedapproximately stationary and then applying either a force in theapproximate direction B to both of the limbs 54, 55 extending from theknot 52, or a force in the approximate direction B to the opening 56. Asdescribed in greater detail below, the Lark's Head knot can be modifiedto form a self-locking knot.

A person skilled in the art will recognize other ways by which a Lark'sHead knot can be formed. Similarly, a person skilled in the art will befamiliar with other types of knots that can be formed in suturefilaments, and will understand ways in which other knots can be adaptedfor use in a manner as the Lark's Head knot is used in the presentdisclosure. The present disclosure is not limited to use only with aLark's Head knot.

The suture filament 50 can be an elongate filament, and a variety ofdifferent types of suture filaments can be used, including but notlimited to a cannulated filament, a braided filament, and a monofilament. The type, size, and strength of the filament can depend, atleast in part, on the other materials of the implant, including thematerial(s) of the cortical button and the ligament graft, the tissue,bone, and related tunnels through which it will be passed, and the typeof procedure in which it is used. In one exemplary embodiment thefilament is a #0 filament (about 26 gauge to about 27 gauge), such as anOrthocord™ filament that is commercially available from DePuy Mitek,LLC., 325 Paramount Drive, Raynham, Mass. 02767, or an Ethibond™filament that is commercially available from Ethicon, Inc., Route 22West, Somerville, N.J. 08876. The thickness of the filament shouldprovide strength in the connection but at the same time minimize thetrauma caused to tissue through which it passes. In some embodiments thefilament can have a size in the range of about a #5 filament (about 20gauge to about 21 gauge) to about a #3-0 filament (about 29 gauge toabout 32 gauge). Orthocord™ suture is approximately fifty-five tosixty-five percent PDS™ polydioxanone, which is bioabsorbable, and theremaining thirty-five to forty-five percent ultra high molecular weightpolyethylene, while Ethibond™ suture is primarily high strengthpolyester. The amount and type of bioabsorbable material, if any,utilized in the filaments of the present disclosure is primarily amatter of surgeon preference for the particular surgical procedure to beperformed. In some exemplary embodiments, a length of the filament canbe in the range of about 0.2 meters to about 5 meters, and in oneembodiment it has a length of about 1.5 meters.

FIG. 4 illustrates one exemplary embodiment of the suture filament 50being associated with the body 10 to form a surgical implant 100′. Asshown, the Lark's Head knot 52 is disposed on a first, top side 10 a ofthe body 10, and the limbs 54, 55 extending therefrom are used toassociate the filament 50 with the body 10. The limbs 54, 55 can beselectively passed through one of the thru-holes 24 to a bottom side 10b of the body 10, and then through another of the thru-holes 24 back tothe top side 10 a. In the illustrated embodiment, the first limb 54passes through the second thru-hole 24 b to reach the bottom side 10 band then through the third thru-hole 24 c to reach the top side 10 a,while the second limb 55 passes through the third thru-hole 24 c toreach the bottom side 10 b and then through the second thru-hole 24 b toreach the top side 10 a, forming a coil or loop 60 a of the first limb54 and a coil or loop 60 b of the second limb 55. The terminal ends 54t, 55 t of the limbs 54, 55 can then be passed through the opening 56defined by the Lark's Head knot 52. As shown, the terminal end 54 t canbe passed from the second side 56 b of the opening 56, as shown a rightside, through the opening 56, and to a first side 56 a of the opening56, as shown a left side, while the terminal end 55 t can be passed fromthe first side 56 a, through the opening 56, and to the second, oppositeside 56 b. The limbs 54, 55 can continue to be pulled through theopening 56 until a desired coil size for each of the first and secondlimbs 54, 55 is achieved. In alternative embodiments, one or both of thelimbs 54, 55 can be passed through the opening 56 multiple times beforeusing the limbs 54, 55 to adjust the coils 60 to the desired size.

Once the terminal ends 54 t, 55 t have been passed through the opening56 and the desired coil size has been achieved, the opening 56 can becollapsed. One way that the opening 56 can be collapsed is by applying aforce to the terminal ends 54 t, 55 t in an approximate direction C asshown, while also applying a counterforce to the coils 60 toapproximately maintain the circumference of the coils. Without thecounterforce, the force in the approximate direction C would typicallydecrease the circumference of the coils 60 before collapsing the opening56. Because the terminal ends 54 t, 55 t are passed through opposingsides 56 a, 56 b of the opening 56, and compression of the Lark's Headknot 52 against a top surface 20 of the body 10 creates resistanceagainst loosening, the resulting collapsed knot is self-locking, meaningthe Lark's Head knot 52 is a sliding knot that locks itself without theaid of additional half-hitches or other techniques known to help securea location of a knot with respect to the body 10.

After the opening 56 is collapsed, a circumference of the coils 60 canagain be decreased by applying force to the terminal ends 54 t, 55 t inthe approximate direction C with the first terminal end 54 t generallycontrolling the size of the coil 60 a and the second terminal end 55 tgenerally controlling the size of the coil 60 b. Because the collapsibleopening 56 is self-locking, it can be more difficult to increase acircumference of the coils 60 a, 60 b after the opening 56 is collapsed.However, a person skilled in the art will understand how portions of thefilament 50 that form the collapsible knot 52 can be manipulated toallow for increases in the circumference of the coils 60 a, 60 b.

In other embodiments, more than one coil can be formed by the first orsecond filament limbs. One exemplary embodiment of such an implant 100″is shown in FIG. 5. Similar to the implant 100′, the Lark's Head knot 52is disposed on the top side 10 a of the body 10, and the limbs 54, 55extending therefrom are selectively passed through multiple thru-holes24 of the body 10 to associate the filament 50 with the body 10. In theillustrated embodiment, the first limb 54 passes distally through thesecond hole 24 b to the bottom side 10 b of the body 10, and through thethird thru-hole 24 c back to the top side 10 a twice to form a firstcoil 60 a and a second coil 60 c before it is then passed through theopening 56 defined by the Lark's Head knot 52 from the second side 56 bof the opening 56 to the first side 56 a. Similarly, the second limb 55passes distally through the third hole 24 c to the bottom side 10 b, andthrough the second thru-hole 24 b back to the top side 10 a twice toform a first coil 60 b and a second coil 60 d before it is then passedthrough the opening 56 from the first side 56 a to the second side 56 b.The opening 56 can be collapsed, and a circumference of the first andsecond coils 60 a, 60 c can be adjusted by the terminal end 54 t and thefirst and second coils 60 b, 60 d can be adjusted by the terminal end 55t in manners similar to those described above with respect to the device100′. The inclusion of a second coil formed from the limbs 54, 55increases the strength of the implant 100″ due to a pulley effect,allowing the implant 100″ to be more stable when it is implanted in boneand to more stably hold a ligament graft attached to one or more of thecoils 60.

Any number of coils can be formed from the first and second limbs 54,55, and the number of coils formed in the first limb 54 does not have tobe the same number of coils formed in the second limb 55. In someexemplary embodiments, three or four coils can be formed in one or bothof the limbs. Further, the limbs used to form the coils can be passedthrough any number of thru-holes formed in the body 10. The first limb54 does not need to pass through the same thru-holes through which thesecond limb 55 passes. Accordingly, by way of non-limiting example, acoil of the first limb 54 can be formed by passing the limb through thefirst thru-hole 24 a and then back through the fourth thru-hole 24 d anda coil of the second limb 55 can be formed by passing the limb throughthe third thru-hole 24 c and then back through the second thru-hole 24b. By way of further non-limiting example, a coil of the first limb 54can be formed by passing the limb through the second thru-hole 24 b andthen back through the fourth thru-hole 24 d and a coil of the secondlimb 55 can be formed by passing the limb through the third thru-hole 24c and then back through the second-thru hole 24 b.

Likewise, when multiple coils are formed in one limb, that limb does nothave to be passed through the same thru-holes to form each coil.Accordingly, by way of non-limiting example, a first coil of the firstlimb 54 can be formed by passing the limb through the second thru-hole24 b and then back through the third thru-hole 24 c and a second coil ofthe first limb 54 can be formed by passing the limb through the firstthru-hole 24 a and then back through the fourth thru-hole 24 d. By wayof further non-limiting example, a first coil of the second limb 55 canbe formed by passing the limb through the fourth thru-hole 24 d and thenback through the first thru-hole 24 a and a second coil of the secondlimb 55 can be formed by passing the limb through the fourth thru-hole24 d and then back through the second thru-hole 24 b. In yet one furthernon-limiting example, a coil of the first limb 54 can be passed throughthe second thru-hole 24 b and then back through the second thru-hole 24b and a coil of the second limb 55 can be passed through the thirdthru-hole 34 c and then back through the third thru-hole 24 c, with thefirst limb 54 and the second limb 55 intersecting at least once on thebottom side 10 b so that the limbs 54, 55 remain on the bottom side 10 bwhen they are passed back through the same thru-hole they came to reachthe bottom side 10 b in the first place. A person skilled in the artwill recognize a number of configurations between the filament andthru-holes that can be used to form one or more coils in the filamentlimbs before disposing terminal ends of the limbs through a collapsibleopening of a knot to create a self-locking knot.

A variety of tests were performed to assess the strength and integrityof an implant having a self-locking knot and four coils like some of theembodiments provided for herein. In particular, the tests were performedon the implant 100 shown in FIG. 2, with the filament being a braided #2ultra high molecular weight polyethylene suture with a loopcircumference of approximately 40 millimeters. Three separate cycletests of varying length were performed. Generally, a cyclical load wasapplied to the implant 100 a plurality of times, with the load cyclingbetween about 50 Newtons and about 250 Newtons. After a certain numberof cycles were performed, the distance a graft migrated from itsoriginal position was measured. After 10 cycles a displacement of theimplant 100 was about 1.0 mm, after 750 cycles a displacement of theimplant was about 1.4 millimeters, and after 1000 cycles a displacementof the implant was about 1.4 millimeters. Further details about testingprotocols of this nature can be found in an article written by Kamelgeret al., entitled “Suspensory Fixation of Grafts in Anterior CruciateLigament Reconstruction: A Biomechanical Comparison of 3 Implants,”published in Arthroscopy, Jul. 25, 2009, pp. 767-776, and in an articlewritten by Petre et al., entitled “Femoral Cortical Suspension Devicesfor Soft Tissue Anterior Cruciate Ligament Reconstruction,” published inThe American Journal of Sports Medicine, February 2013, pp. 416-422, thecontent of each which is incorporated by reference herein in itsentirety. A person skilled in the art will recognize that the testresults are dependent at least on the type and size of the filament ofthe implant.

Another test determined an ultimate failure load of the implant 100. Theultimate failure load measures the load at which the implant 100 fails.The ultimate failure load tested for the implant 100 was about 1322Newtons. During the ultimate failure load test, the displacement at 450Newtons was also measured, with displacement being about 2.0millimeters. Still another test performed on the implant was aregression stiffness test, which plots the displacement of the implantin comparison to the load and a slope of the initial line is measured.The implant 100 demonstrated a regression stiffness of about 775 Newtonsper millimeter. Again, a person skilled in the art will recognize thatthese test results are dependent at least on the type and size of thefilament of the implant.

FIGS. 6A and 6B illustrate the ability to selectively control some coils60 a′, 60 c′ of an implant 100′″ using one limb 54′ and other coils 60b′, 60 d′ of the implant 100′″ using the other limb 55′. As shown, theimplant 100′″ includes a single filament 50′ associated with a body 10′having a plurality of thru-holes 24′ formed therein. The configurationbetween the filament 50′ and the body 10′ is similar to the implants100, 100″ described above with respect to FIGS. 2 and 5. As shown, aself-locking knot 52′ is formed on a top side 10 a′ of the body 10′ andfour coils 60′ are formed from first and second limbs 54′, 55′ extendingfrom the self-locking knot 52′, the four coils 60′ being substantiallydisposed on a bottom side 10 b′ of the body 10′. Terminal ends 54 t′, 55t′ of the first and second limbs 54′, 55′ pass through an opening 56′ ofthe self-locking knot 52′ before the knot is collapsed, and can be usedto adjust a circumference of the coils 60′. In the illustratedembodiment, the first limb 54′ is differentiated from the second limb55′ by including markings on the first limb 54′. These visual indicatorsallow a surgeon to easily know which coils are controlled by whichlimbs, and can be added to the filament before or after the filament isassociated with the body 10′.

In the illustrated embodiment, a first ligament graft 102′ is coupled tofirst and second coils 60 a′, 60 c′ of the first limb 54′ by wrappingthe graft 102′ through each of the first and second coils 60 a′, 60 c′,and a second ligament graft 104′ is coupled to first and second coils 60b′, 60 d′ of the second limb 55′ by wrapping the graft 104′ through eachof the first and second coils 60 b′, 60 d′. As shown in FIGS. 6A and 6B,applying a force to the first limb 54′ in an approximate direction Ddecreases the circumference of the first and second coils 60 a′, 60 c′,thereby drawing the first ligament graft 102′ closer to the body 10′.More particularly, as tension is created by the force, the circumferenceof the diameter of the second coil 60 c′ decreases and advances thefirst graft 102′. As the distance between distal ends of the second coil60 c′ and the first coil 60 a′ increases, the weight of the graft 102′helps create a counterforce that maintains the circumference of thesecond coil diameter while the circumference of the first coil 60 a′decreases to catch-up to the second coil 60 c′ and the graft 102′. Aperson skilled in the art will understand how the application of variousforces and tensions to the first and second limbs 54′, 55′, the firstand second coils 60 a′, 60 c′ and 60 b′, 60 d′, and the first and secondgrafts 102′, 104′ associated therewith can be manipulated to selectivelyadjust locations of the grafts 102′, 104′ with respect to the body 10′.

As a result of this configuration, one ligament graft can be pulledcloser the body 10′ than another ligament graft. Such graftconfigurations can be useful to surgeons. By way of non-limitingexample, if during the course of a tissue repair the surgeonaccidentally amputated one of the hamstring tendons during harvesting orgraft preparation, the coils associated with one of the terminal endscan be adjusted so that the longer tendon is pulled deeper into thefemoral tunnel with the shorter tendon being more proximal of the longertendon, thus leaving more graft for the tibial tunnel. By way of furthernon-limiting example, grafts can be independently tensioned such thatthey are tightest at different angles of knee flexion, which can providesuperior biomechanics due to the repair being more anatomic. Otherconfigurations that can permit selective, independent tightening of thecoils formed in the suture filament can also be used while maintainingthe spirit of the present disclosure. For example, two separate knot orfinger-trap mechanisms can be disposed through the same thru-holes inthe button to permit selective, independent control of the coils.

Four non-limiting alternative embodiments for associating a suturefilament 150, 250, 950, 950′ with a cortical button 110, 210, 910, 910′to form an implant 200, 300, 900, 900′ are illustrated in FIGS. 7A-7E,FIGS. 11A-11H, FIGS. 9A-9B, and FIG. 10 respectively. Further, FIGS.8A-D illustrate an embodiment for associating a suture filament 850 withan implant 870. Starting first with FIGS. 7A-7E, the cortical button 110includes four thru-holes 124 disposed therein and the suture filament150 is a braided suture. After forming a pretzel-shaped knot 152 usingtechniques known to those skilled in the art, first and second terminalends 154 t, 155 t of the filament 150 can be passed through the twointerior thru-holes 124 of the body 110, as illustrated in FIG. 7A, toform two loops or coils 160 a, 160 b for receiving a ligament graft. Inthis embodiment, both the first and second limbs 154, 155 pass throughthe same interior thru-hole 124 to pass from a top side 110 a to abottom side 110 b of the body 110. Likewise, both limbs 154, 155 passthrough the same interior thru-hole 124 to pass from the bottom side 110b back to the top side 110 a.

As shown in FIG. 7B, the terminal ends 154 t, 155 t can be passedthrough openings of the pretzel-shaped knot 152. Other suitable slidingknots can be used in lieu of a pretzel-shaped knot. Subsequently, aforce can be applied to the terminal ends 154 t, 155 t in an approximatedirection E to collapse and advance the knot 152 towards a top surface120 of the body 110, as shown in FIG. 7C. The pretzel knot 152 is notgenerally self-locking. Accordingly, as shown in FIG. 7D, one or morehalf-hitches 161 can be formed in the terminal ends 154 t, 155 t tosecure and lock a location of the collapsed pretzel knot 152 withrespect to the body 110. A graft 202 can then be disposed withinopenings of the coils 160 a, 160 b formed by the first and second limbs154, 155, as shown in FIG. 7E.

Tests performed using an implant like the embodiment shown in FIG. 7E,the filament being a braided #5 ultra high molecular weight polyethylenesuture with a loop circumference of approximately 40 millimeters,yielded a 10^(th) cycle displacement of approximately 1.9 millimeters, a750^(th) cycle displacement of approximately 2.2 millimeters, and a1000^(th) cycle displacement of approximately 2.3 millimeters. Theultimate failure load was measured to be approximately 1521 Newtons.Displacement at a load of 800 Newtons was measured to be approximately4.1 millimeters. Meanwhile, the regression stiffness was determined tobe approximately 267 Newtons per millimeter. A person skilled in the artwill recognize that the test results are dependent at least on the typeand size of the filament of the implant.

While the present disclosure provides the formation of a variety ofknots that can be used in conjunction with surgical implants, FIGS. 8A-Dillustrate one exemplary embodiment of a knot formation that isparticularly strong and has a particularly low profile. In theillustrated embodiment, a suture 850 is tied directly onto an implanthaving no holes formed therein because the illustrations are intended tofocus on the knot formation. A person having ordinary skill in the artwill understand how to incorporate the knot formation into a corticalbutton or other implants in view of the present disclosure.

As shown in FIG. 8A, suture 850 can be formed into a pretzel, oroverhand, cinch knot 852 having suture limbs 854, 855 extendingtherefrom. The knot 852 can have three collapsible openings 852 a, 852b, and 852 c. In the illustrated embodiment of FIG. 8A, the firstcollapsible opening 852 a is in a central location of the knot 852, andthe second and third collapsible openings 852 b, 852 c are located onopposite sides from the first collapsible opening 852 a.

An implant 870 can be placed over the suture limbs 854, 855 such thatthe suture limbs can be wrapped around the implant 870 from a top side870 a to a bottom side 870 b of the implant 870, thereby creating firstand second filament loops, or coils, 860 a, 860 b, respectively. Theterminal ends (not visible) of the suture limbs 854, 855 are then passedthrough the first collapsible opening 852 a from a front side of theknot 852 to a rearward side of the knot, as shown in FIG. 8B.

The suture limbs 854, 855 are next passed from the top side 870 a of theimplant 870 around the implant 870 to the bottom side 870 b of theimplant 870 and back up to the top side 870 a of the implant 870 tocreate the third and fourth filament loops 860 c, 860 d, respectively,as shown in FIG. 8C. The terminal ends of the suture limbs 854, 855 arethen passed through the second and third collapsible openings 852 b, 852c, respectively.

The knot 852 can be cinched down using any technique known to thoseskilled in the art or otherwise provided for in any embodiment of thepresent disclosure. In the illustrated embodiment, to effectivelyillustrate the low profile of the knot when fully cinched, the loops 860a-860 d are collapsed around the implant 870 as shown in FIG. 8D.Collapsing of the knot 852 and the loops 860 a-860 d can be achieved,for example, by maintaining tension on the limbs 854, 855 in thedirections R, S, respectively, while applying tension to the loops 860a-860 d in the opposite directions, R′, S′. The loops 860 a-860 d can beoperated in a manner similar to loops of other configurations providedfor herein, including but not limited to loops 60 a-60 d, 60 a′-60 d′,160 a and 160 b, 260 a and 260 b, 360, 460 a and 460 b, 560 a-560 d, 660a-660 d, 760 a and 760 b, and 760 a′-760 d′, and thus graft 870 can beinserted within an opening(s) 861 a-861 d defined by the loop(s) 860a-860 d even if the loops 860 a-860 d are collapsed tightly around theimplant 870 as shown in FIG. 8D. Likewise, while FIG. 8D illustrates theloops 860 a-860 d are collapsed around the implant 870, in otherembodiments, one or more of the loops 860 a-860 d can not be fullycollapsed, such as described with respect to the many implants providedfor herein (e.g., by way of non-limiting examples, implants 100′, 200).Further, the knot configuration as illustrated by FIGS. 8A-8D can beused in the other configurations of implants provided for herein orotherwise known to those skilled in the art.

Further, in yet other embodiments, any multiple of loops can be createdby passing the suture limbs 854, 855 around the implant 870 as manytimes as needed. Further still, the suture limbs can be passed throughany of the collapsible openings 852 a-852 c in any order when creatingthe filament loops 860 a, 860 b, 860 c, 860 d. By way of non-limitingexamples, two limbs can be passed through openings 852 b or 852 cinstead of opening 852 a, and/or the limbs can be passed throughdifferent openings during both passes instead of the same opening duringone pass.

FIGS. 9A and 9B illustrate the knot formation of FIGS. 8A-8D being usedwith an implant 900 that includes a cortical button 910. The button 910has at least two through holes 924 b, 924 c disposed therein and asuture filament 950 (e.g., a braided suture) associated with the button910 to form the implant 900. Similar to the suture 850, the filament 950can be formed into a pretzel shaped, or overhand, knot 952. The knot 952can be disposed on a top side 910 a of the button 910, and can have atleast three collapsible openings 952 a, 952 b, and 952 c. As shown, thefirst collapsible opening 952 a can be located in a central location ofthe knot 952, and the second and third collapsible openings 952 b, 952 ccan be located on opposite sides from the first collapsible opening 952a.

The knot 952 can have limbs 954, 955 extending therefrom that can beselectively passed through thru-holes 924 a-d to associate the filament950 with the button 910. In the illustrated embodiment of FIG. 9A, thefirst limb 954 passes distally through the third hole 924 c to thebottom side 910 b of the button 910, and through the second hole 924 bback to the top side 910 a to form a first filament loop, or coil, 960a. Similarly, the second limb 955 passes distally through the secondhole 924 b to the bottom side 910 b of the button 910, and through thethird hole 924 c back to the top side 910 a to form a second filamentloop 960 b.

When both the first and second limbs 954, 955 are on the top side 910 aof the button 910, they can then be passed through a first opening 952 aof the overhand knot 952. As shown, the first limb 954 is then passeddistally through the fourth hole 924 d to the bottom side 910 b of thebutton 910, and then through the first hole 924 a back to the top side910 a to form a third coil 960 c. Likewise, the second limb 955 ispassed distally through the first hole 924 a to the bottom side 910 b ofthe button 910, and through the fourth hole 924 d back to the top side910 a to form a fourth coil 960 d. The terminal end 954 t of the firstlimb 954 can then be passed through the second collapsible opening 952b, and the terminal end 955 t of the second limb 955 can be passedthrough the third collapsible opening 952 c. As discussed above, theorder and placement of the limbs 954, 955 through the openings 952 a,952 b, and 952 c, can be altered as desired without departing from thespirit of the present disclosure.

The knot 952 can be collapsed onto the suture limbs 954, 955 passingtherethrough by application of a force F_(C) on the filament loops 960a-960 d, as shown in FIG. 9A, while maintaining tension on the first andsecond limbs 954, 955. A circumference of the first and third coils 960a, 960 c can be adjusted by application of a pulling force F_(P) on theterminal end 954 t, and likewise, a circumference of the second andfourth coils 960 b, 960 d can be adjusted by application of the pullingforce F_(P) on the terminal end 955 t in manners similar to thosedescribed above. The inclusion of a second coil formed from each of thelimbs 954, 955 increases the strength of the implant 900 due to a pulleyeffect, allowing the implant 900 to be more stable when it is implantedin bone and to more stably hold a ligament graft 970 attached throughthe filament loops 960 a-960 d. Once the filament loops 960 a-960 d arecollapsed to the desired lengths, the knot 952 is collapsed, the suturelimbs 954, 955 can be tied with a half hitch knot proximate to the knot952 to maintain a location of the knot 952 with respect to the button910, and then the suture limbs 954, 955 can be cut to length. The fourloops 960 a-960 d can maintain a combined average maximum loading of atleast about 765 N once implanted, with the strength being supplied, atleast in part, by the knot configuration.

One advantage of passing the suture limbs 954, 955 through each openingof the overhand knot 952 is that each collapsible opening 952 a-952 c ofthe knot 952 is able to engage more surface area of the portion of thesuture limbs 954, 955 passing therethrough. This additional surface areacontact between the collapsible openings 952 a-952 c and the suturelimbs 954, 955 creates a more secure cinch. Additionally, anotheradvantage of passing the suture limbs 954, 955 through each opening ofthe overhand knot 952 is a reduction in binding of the knot 952 ascompared to the suture limbs being threaded through a single opening ofthe knot. Still further, by including at least the four filament loops960 a-960 d, the load applied by the ligament implant 970 is betterdispersed and therefore there is a reduction in cyclic displacement ascompared to using only two filament loops. A further advantage is theresulting knot 952 can have a lower profile as compared to a knot whereeach limb is passed through a single opening of the knot.

Any number of filament loops can be formed from the first and secondlimbs 954, 955 to hold any number of ligament implants 970, and thenumber of filament loops formed with the first limb 954 does not have tobe the same as the number of filament loops formed by the second limb955. In some embodiments, three or four filament loops can be formed byone or both of the limbs 954, 955. Further, the limbs used to form thefilament loops can be passed through any number of thru-holes formed inthe button 910. The first limb 954 does not need to pass through thesame collapsible opening through which the second limb 955 passes.Likewise, when multiple filament loops are formed with one limb, thatlimb does not have to be passed through the same thru-holes to form eachcoil. Moreover, the first limb 954 and the second limb 955 need not passthrough the collapsible openings 952 a-c in the order prescribed above.For example, the suture limbs 954, 955 can first pass throughcollapsible opening 952 b, then separately through collapsible openings952 a and 952 c. A person skilled in the art will recognize a number ofconfigurations between the filament and thru-holes that can be used toform one or more coils in the filament limbs before disposing terminalends of the limbs through the collapsible openings 952 a-c of the knot952 in any order.

One example of an alternate configuration is shown in the embodiment ofFIG. 10. Similar to the implant 900, a suture 950′ can be formed into apretzel shaped, or overhand, knot 952′ disposed on a top side 910 a′ ofthe body 910′. The knot 952′ can have three collapsible openings 952 a′,952 b′, and 952 c′. The suture configuration of the implant 900′ issimilar to that of the implant 900 of FIGS. 9A and 9B, however, insteadof threading suture limbs through four of the openings in the corticalbutton, only two openings are used. In some embodiments, the body mayonly include two openings. As shown, limbs 954′, 955′ of the suture 950′can extend from the knot 952′ and can be selectively passed through afirst thru-hole 924 b′ to a bottom side 910 b′ then through a secondhole 924 c′ to associate the filament 950′ with the body 910′. In theillustrated embodiment of FIG. 10, the first limb 954′ passes distallythrough the second hole 924 b′ to the bottom side 910 b′ of the body910′, and through the third hole 924 c′ back to the top side 910 a′ toform a first filament loop 960 a′. Similarly, the second limb 955′passes distally through the third hole 924 c′ to the bottom side 910 b′of the body 910′, and through the third hole 924 c′ back to the top side910 a′ to form a second filament loop 960 b′.

When both the first and second limbs 954′, 955′ are on the top side 910a′ of the button 910′, they can be passed through a first opening 952 a′of the overhand knot 952′. The first limb 954′ can then pass distallythrough the second hole 924 b′ to the bottom side 910 b′ of the body910′, and through the third hole 924 c′ back to the top side 910 a′ toform a third filament loop 960 c′. Likewise, the second limb 955′ canpass distally through the third hole 924 c′ to the bottom side 910 b′ ofthe body 910′, and through the second hole 924 b′ back to the top side910 a′ to form a fourth filament loop 960 d′. The terminal end 954 t′ ofthe first limb 954′ can then be passed through the second collapsibleopening 952 b′, and the terminal end 955 t′ of the second limb 955′ canbe passed through the third collapsible opening 952 c′. The knot 950′can be collapsed onto the suture limbs 952′, 954′ passing therethroughby application of a force F_(c)' on the filament loops 960 a′-960 d′,while maintaining tension on the first and second limbs 954′, 955′. Acircumference of the first and second coils 960 a′, 960 c′ can beadjusted by the terminal end 954 t′ and the third and fourth coils 960b′, 960 d′ can be adjusted by the terminal end 955 t′ in manners similarto those described above. Further, any number of loops and anyconfigurations with respect to the body 910 can be used. Still further,any combination of passing the limbs 954′, 955′ through the openings 952a′, 952 b′, 952 c′, as described above, can be used for this describedembodiment without departing from the spirit of this disclosure.

The embodiment illustrated in FIGS. 11A-11H also include a corticalbutton 210 having at least three thru-holes 224 a, 224 b, 224 c disposedtherein and a suture filament 250 that is a braided suture associatedwith the button 210 to form an implant 300. As shown in FIG. 11A, aterminal end 254 t of a first limb 254 is passed from a top side 210 ato a bottom side 210 b of the body 210 through one of the thru-holes 224a and a terminal end 255 t of a second limb 255 is passed from the topside 210 a to the bottom side 210 b through another thru-hole 224 b. Thetwo terminal ends 254 t, 255 t are then both passed back to the top side210 a through the third thru-hole 224 c, as shown in FIG. 11B. Theresulting configuration is a first loop 263 formed on the top side 210 afrom a central portion 250 c of the filament 250 at an approximatemidpoint 250 m of the filament 250, and first and second coils 260 a,260 b primarily located below the bottom side 210 b.

As shown in FIG. 11C, the terminal ends 254 t, 255 t can be formed intoa sliding knot 252 such as a Buntline Hitch knot using techniques knownto those skilled in the art. Other suitable sliding knots can be used inlieu of the Buntline Hitch knot. A force can then be applied in anapproximate direction F to the terminal ends to tighten the BuntlineHitch knot, and as shown in FIG. 11D, the stationary terminal end, asshown the terminal end 254 t, can be cut so that it is substantiallyshorter than the sliding terminal end extending proximally from thetightened sliding knot 252, as shown the terminal end 255 t. The thirdthru-hole 224 c can be sized such that the Buntline Hitch knot is toobig to pass through it. Thus, a force in an approximate direction G canbe applied to the longer sliding terminal end 255 t to advance the knot252 toward the body 210, and to collapse the first loop 263 against thetop surface 220 of the body 210, as shown in FIG. 11E.

Optionally, a secondary loop 280 can be added to the first and secondcoils 260 a, 260 b, as shown in FIG. 11F. As shown, the secondary loop280 is a closed, fixed loop having an approximately fixed circumference.The secondary loop 280 can be formed using any number of techniquesknown to those skilled in the art, but in the illustrated embodiment thesecondary loop is disposed around the first and second coils 260 a, 260b and tied together to form the closed, fixed loop. As shown in FIG.11G, a ligament graft 302 can be disposed around the secondary loop 280.While in other embodiments the ligament graft was only disposed aroundthe loop once, FIG. 11G illustrates that ligament grafts 302 can bedisposed around a filament in any of the embodiments described hereinmultiple times. A force in an approximate direction H can then beapplied to the long remaining terminal end 255 t to decrease thecircumference of the first and second coils 260 a, 260 b and advance theligament graft 302 closer to the body 210, as shown in FIG. 11H.

In the embodiment illustrated in FIGS. 11A-11H, the ligament graft isnot attached directly to coils 260 a, 260 b formed by the filament 250,but instead is coupled to the secondary loop 280. Such a secondary loopcan be used in any of the embodiments described or derivable fromdisclosures made herein. In some embodiments the secondary loop can helpminimize accidental graft damage due to wear with the main suturefilament when the circumferences of the coils of the main filament areadjusted.

In some embodiments, including but not limited to those implants havinga self-locking knot, a sleeve or spacer can be disposed over a portionof the first and second limbs on the top side of the body, adjacent tothe top surface. The optional sleeve can assist in preventing a surgeonfrom cutting terminal ends of the limbs extending proximally from theknot too close to the body. The integrity of the knot, and thus thestrength of the implant, can be compromised when the terminal ends ofthe limbs are cut too close to the body. The sleeve can generally haveelastic properties such that it bunches as compressive forces areapplied, and a surgeon can then cut the terminal ends at a locationproximal of the sleeve.

As shown in FIG. 12, in one exemplary embodiment of an implant 400formed by a body 310 and a suture filament 350 forming both aself-locking knot 352 on a top side 310 a of the body 310 and aplurality of coils 360 substantially disposed on a bottom side 310 b ofthe body 310, sleeve 358 is a single suture filament having a pluralityof bores formed therein to thread first and second limbs 354, 355through the sleeve 358. The sleeve 358 can be disposed around a portionof the first limb 354 on the top side 310 a, wrap around a bottomsurface 322 of the body 310, and then wrap back around to the top side310 a so it can be disposed around a portion of the second limb 355.Wrapping the sleeve 358 around the bottom surface 322 can help minimizeproximal movement of the sleeve 358, toward the terminal ends 354 t, 355t when the limbs 354, 355 are tightened. The first terminal end 354 tpasses into the sleeve 358 at a first bore 358 a and out of the sleeveat a second bore 358 b, while the second terminal end 355 t passes intothe sleeve 358 at a third bore 358 c and out of the sleeve at a fourthbore 358 d. As shown, free ends 358 e, 358 f of the sleeve 358 canextend proximally from the second and fourth bores 358 b, 358 d.

In other embodiments, the free ends 358 e, 358 f can be eliminated, orthe sleeve can be configured such that the free ends extend distally.The implant 100 of FIG. 1B is an example of an embodiment that does notinclude free ends. Rather, the first and second terminal ends passinto/out of the sleeve 58 at terminal ends 58 t ₁, 58 t ₂ of the sleeverather than at first and fourth bores. In still other embodiments,separate sleeves can be disposed on each of the first and second limbs.In such embodiments, the only bores formed in the sleeves may be thoseformed at the respective terminal ends, and thus the first and secondterminal ends of the filament can pass into and out of the sleevesthrough the terminal ends of the sleeves. In still further embodiments,the first and second terminal ends can extend through the same sleeve,or alternatively, free ends of the sleeve can be connected together toform a continuous loop. In addition to or in lieu of other sleeveconfigurations, other components configured to assist in allowing asurgeon to know where to cut the terminal ends after they are no longerneeded can also be incorporated into the implants described hereinwithout departing from the spirit of the disclosure.

The sleeve can be made from a wide variety of biocompatible flexiblematerials, including a flexible polymer, or it can be another filament.In one embodiment the sleeve is made of a polymeric material. In anotherembodiment, the sleeve is a flexible filament, such as a braided suture,for example Ethibond™ #5 filament. If the sleeve is formed from ahigh-strength suture such as Orthocord™ #2 filament, the braid can berelaxed by reducing the pick density. For example, Orthocord™ #2filament, which is typically braided at sixty picks per 2.54 centimeterscan be braided at approximately thirty to forty picks per 2.54centimeters, more preferably at about 36 picks per 2.54 centimeters. Ifthe sleeve material is formed about a core, preferably that core isremoved to facilitate insertion of the filament limbs, which maythemselves be formed of typical suture such as Orthocord™ #0 suture or#2 suture braided at sixty picks per 2.54 centimeters.

A length and diameter of the sleeve can depend, at least in part, on thesize and configuration of the components of the construct with which itis used and the surgical procedure in which it is used. In embodimentsin which the sleeve is a filament, a size of the sleeve can be in therange of about a #7 filament (about 18 gauge) to about a #2-0 filament(about 28 gauge), and in one embodiment the size can be about a #5filament (about 20 gauge to about 21 gauge). In addition, the sleeve canbe thickened by folding it upon itself coaxially, (i.e., sleeve in asleeve). A person having skill in the art will recognize comparablediameters that can be used in instances in which the sleeve is made of apolymeric or other non-filament material. In embodiments in which asingle sleeve is disposed over portions of both the first and secondterminal ends, a length of the sleeve can be in the range of about 1centimeter to about 12 centimeters, and in one embodiment the length canbe about 5.5 centimeters. In embodiments in which separate sleeves aredisposed over portions of the first and second terminal ends, a lengthof each sleeve can be in the range of about 0.5 centimeters to about 6centimeters, and in one embodiment each has a length of about 2.5centimeters. The axially compressible nature of the sleeves can be suchthat a length of the portion of the sleeve disposed on one of the limbscan compress fully to a length that is in the range of about one-half toabout one-eighth the original length of that portion of the sleeve, andin one exemplary embodiment it can compress to a length that is aboutone-fifth the original length of that portion of the sleeve. Thus, ifthe length of the sleeve disposed around the first limb is approximately3 centimeters, when fully compressed the sleeve can have a length thatis approximately 0.6 centimeters.

In some embodiments, a second suture filament can be associated with thebody of the implant to help guide or shuttle the filament during asurgical procedure. As shown in FIG. 13, an embodiment of an implant 500includes a body 410 having two thru-holes 424 formed therein and a firstsurgical filament 450 coupled thereto. In the illustrated embodiment,rather than having a knot formed on a top side 410 a of the body 410,limbs 454, 455 of the first surgical filament 450 are intertwined arounda mid-portion 450 m of the filament 450 on the top side 410 a, therebyforming an intertwining configuration 452. The first and second limbs454, 455 can also extend distally from the intertwining configuration452. More particularly, the limbs 454, 455 can extend through thethru-holes 424 a plurality of times to form a plurality of coils 460 a,460 b substantially disposed on a bottom side 410 b of the body 410. Thefriction resulting from the intertwining configuration 452 can besufficient to assist in retaining sizes and positions of the coils 460a, 460 b, and to minimize any slipping associated therewith.

A second suture filament or shuttle filament 490 can be disposedlongitudinally through the body as shown, for instance in a longitudinalbore 425 formed therethrough. The filament can extend substantiallyalong a central, longitudinal axis L of the body 410, and thus canextend through the thru-holes 424 formed in the body 410, resulting in aleading end 490 a and a trailing end 490 b. A knot 492 or otherprotrusion larger than a diameter of the longitudinal bore 425 can beformed in or otherwise located on the trailing end 490 b and can assistthe leading end 490 a and the trailing end 490 b in serving as a guideor shuttle for the implant 500, as described in greater detail belowwith respect to FIGS. 16A-16H. By using a single suture disposed throughthe longitudinal bore 425 to serve as a shuttle, the number of suturesused in the system can be reduced, thereby simplifying the procedurewithout diminishing the tactile feedback available to the surgeon oncethe body 410 has flipped on the femoral cortex.

Although the illustrated bore 425 extends through the body 410 andthrough each of the thru-holes 424, a person skilled in the art willrecognize other configurations that can be formed without departing fromthe spirit of the present disclosure, such as having the thru-holes 424situated off-center of the body 410 so they are not intersected by thebore 425, or the bore 425 having a path that does not necessarily extendthrough each thru-hole 424 or all the way through the body 424.Additionally, in some embodiments the longitudinal bore 425 can beformed with an invagination (not shown) on a trailing end 418 of thebody 410 such that it has a diameter that is approximately larger thanthe diameter of the bore 425 and approximately smaller than the diameterof the knot 492. As a result, the knot 492 can be partially fit insidethe body 410 and remain engaged with the body 410 even after the bodyhas been flipped onto the femoral cortex. Once the body 410 is rotatedthrough a specific angle, the knot 492 can disengage with theinvagination and the filament 490 can easily be removed from thepatient. A person having skill in the art will recognize that the sizeand depth of the invagination can control, at least in part, the releaseangle.

A person skilled in the art will recognize that one or more additionalfilaments, like the second filament 490, can be associated with avariety of implant configurations, including configurations describedherein or derivable therefrom. Two further non-limiting examples ofimplants having second suture filaments for shuttling are illustrated inFIGS. 11A and 11B and 12A and 12B.

The implant 600 of FIGS. 14A and 14B includes a body 510 having twothru-holes 524 formed therein and a first surgical filament 550 coupledthereto. The surgical filament 550 is similar to the surgical filament50 of FIG. 5 in that limbs 554, 555 of the filament 550 are used to forma self-locking knot 552 disposed on a top side 510 a of the body 510 andfour coils 560 a, 560 b, 560 c, and 560 d that pass through thethru-holes 524 and are substantially disposed on a bottom side 510 b ofthe body 510. First and second terminal ends 554 t, 555 t of the limbs554, 555 can extend proximally from the self-locking knot 552 and can beused at least to adjust sizes of the coils 560 a, 560 b, 560 c, and 560d in manners consistent with descriptions contained herein. A secondsuture filament or shuttle filament 590 can be disposed longitudinallythrough a longitudinal bore 525 formed in the body 510 along a central,longitudinal axis M, and thus can extend through the thru-holes 524formed in the body 510. Similar to the implant 500 of FIG. 13, a knot592 larger than a diameter of the longitudinal bore 525 can be formed ina trailing end 590 b of the second filament 590 and can assist a leadingend 590 a and the trailing end 590 b in serving as a guide or shuttlefor the implant 600.

The implant 700 of FIGS. 15A and 15B includes a body 610 having fourthru-holes 624 formed therein and a first surgical filament 650 coupledthereto. As shown, the four thru-holes 624 include two inner thru-holes624 b and 624 c that can be used to receive the filament 650 and twoouter thru-holes 624 a and 624 d that can be used to receive shuttlefilaments. As shown, the outer thru-holes 624 a, 624 d can be disposedcloser to leading and trailing ends 616 and 618, respectively, than tothe inner thru-holes 624 b and 624 c, and thus the four thru-holes 624are not approximately equally spaced apart with respect to each other.As also shown, diameters of the two inner holes 624 b and 624 c arelarger than diameters of the two outer holes 624 a and 624 d. Thesurgical filament 650 is similar to the surgical filament 50 of FIG. 5in that first and second limbs 654, 655 of the filament 650 are used toform a self-locking knot 652 disposed on a top side 610 a of the body610 and four coils 660 a, 660 b, 660 c, and 660 d that pass through thethru-holes 624 b, 624 c and are substantially disposed on a bottom side610 b of the body 610. First and second terminal ends 654 t, 655 t ofthe limbs 654, 655 can extend proximally from the self-locking knot 652and can be used at least to adjust sizes of the coils 660 a, 660 b, 660c, and 660 d in manners consistent with descriptions contained herein.As shown, a second, leading suture filament or leading shuttle filament690 can be disposed through the outer thru-hole 624 d and around theleading end 616, and a third, trailing shuttle filament 691 can bedisposed through the outer thru-hole 624 a and around the trailing end618. As described below with respect to aspects of FIGS. 16A-16H, theshuttle filaments 690 and 691 can serve as a guide or shuttle for theimplant 700 to assist in passing the implant 700 through a bone tunnel.

Similar to other filaments of the present disclosure, a shuttle filamentcan be an elongate filament of a variety of types, including but notlimited to a cannulated filament, a braided filament, and a monofilament. The type, size, and strength of the filament can depend, atleast in part, on the other materials of the implant, such as thecortical button, and the type of procedure in which it is used. In oneexemplary embodiment the second suture filament is formed from a #5filament (about 20 gauge to about 21 gauge). In some embodiments thefilament can have a size in the range of about a #2-0 filament (about 28gauge) and about a #5 filament (about 20 gauge to about 21 gauge). Alength of the filament can be in the range of about 0.1 meters to about1.5 meters, and in one embodiment the length is about 1 meter.

Different exemplary features associated with performing an ACL repairusing a surgical implant like those described herein are illustrated inFIGS. 16A-16H. The implant 800 illustrated in FIGS. 16A and 16D-Ggenerally includes thru-holes 724 (not shown) formed therein and a firstsurgical filament 750 coupled thereto. As shown, first and second limbs754, 755 (FIGS. 16F and 16G) of the first surgical filament 750 can beused to form a self-locking knot 752 disposed on a top side 710 a of thebody 710 and a plurality of coils—as shown two coils 760 a, 760 b, butany number of coils can be formed in accordance with the teachingsherein—that pass through the thru-holes 724 and are substantiallydisposed on a bottom side 710 b of the body. Extending proximally fromthe knot can be first and second terminal ends 754 t, 755 t of the limbs754, 755, which can be used at least to adjust sizes of the coils 760 a,760 b in manners consistent with descriptions contained herein. One ormore additional filaments can be associated with the leading and/ortrailing ends 716, 718 of the body 710. As shown, a second filament 790is associated with the leading end 716, and a third filament 791 isassociated with the trailing end 716. A graft 802 can be associated withthe coils 760 a, 760 b using techniques known to those skilled in theart.

A surgeon can begin the procedure by preparing the knee 1000 and softtissue tendon grafts using techniques known by those skilled in the art.As shown in FIG. 16A, a bone tunnel 1002 can be formed in a femur 1001and tibia 1003, with a femoral tunnel 1004 of the bone tunnel 1002including a main channel 1005 and a passing channel 1007, the passingchannel 1007 having a smaller diameter than the main channel 1005, andthe femoral tunnel 1004 being in direct communication with a tibialtunnel 1006 disposed in the tibia 1003. The implant 800 can beintroduced into the tibial tunnel 1006 by applying a force in anapproximate direction J to the second and third suture filaments 790,791, which both extend toward the femoral tunnel as shown. The terminalends 754 t, 755 t can also extend toward the femoral tunnel, such thatsix strands of suture all extend out of the femoral tunnel 1004,proximal of the bone tunnel 1002.

FIGS. 16B and 16C illustrate example orientations for implants 700 and600 of FIGS. 15A and 15B and FIGS. 14A and 14B, respectively, if theywere to be inserted into the bone tunnel 1002 in a manner similar to theimplant 800. As illustrated in FIG. 16B, all six terminal ends of thefilaments 650, 690, and 691 associated with the body 610 can extendproximally when inserted through the bone tunnel 1002 (not shown). Theseterminal ends include the first and second terminal ends 654 t, 655 t ofthe first filament 650, first and second terminal ends 689 t, 690 t ofthe leading shuttle filament 690, and first and second terminal ends 691t, 692 t of the trailing shuttle filament 692. Similarly, as illustratedin FIG. 16C, all four terminal ends of the filaments 550 and 590associated with the body 510 can extend proximally through the bonetunnel 1002 (not shown). These terminal ends include the first andsecond terminal ends 554 t, 555 t of the first filament 550 and firstand second terminal ends 589 t, 590 t of the shuttle filament 590.Grafts 702, 602 can be associated with coils 660, 550 of the implants700, 600 using techniques known to those skilled in the art. Further, aperson skilled in the art will recognize that as the implants 700, 600are inserted into the bone tunnel, filaments and grafts located on thetop and bottom sides 610 a, 510 a and 610 b, 510 b, respectively, can beflexible to allow the construct to be disposed in the tunnel, similar tothe implant 800 of FIG. 16A.

Turning back to the implant 800, as shown in FIG. 16D, a force in theapproximate direction J can be applied to terminal ends 790 t, 791 t ofthe second and third filaments 790, 791, as well as to the terminal ends754 t, 755 t of the first and second limbs 754, 755, to advance eachthrough the tibial tunnel 1006 and into the femoral tunnel 1004. Acounterforce can be applied to the graft 802 so that the entireconstruct is not fully inserted into the bone tunnel 1002, as inexemplary embodiments the graft 802 can be used to help orient thecortical button 710 with respect to the bone tunnel 1002. Further, asthe body 710 and coils 760 a, 760 b enter the bone tunnel 1002, care canbe taken to prevent the body 710 from becoming wrapped in the coils 760a, 760 b. Once the implant 800 enters the bone tunnel 1002, scopes canbe used to continue to monitor it. If the coils 760 a, 760 b undesirablywrap around the body 710, the surgeon can use instruments to unwrap thecoils 760 a, 760 b from the body 710 and/or the surgeon can selectivelyapply tension to the second and third suture filaments 790, 791 and thegraft 802 to manipulate the cortical button 710.

Continued application of the force in the approximate direction J canpull the body 710 through the passing channel 1007. As the body 710passes through the passing channel 1007 and crests while passing out ofthe channel, i.e., when a substantial portion of the body is disposedoutside of the channel, as shown in FIG. 16E, the surgeon can prepare toorient or manipulate the body so that it flips or changes orientation.Because tissue and ligaments can be located near the proximal end of thefemoral tunnel 1004, typically when cortical buttons pass out of afemoral tunnel, the extra tissue can make it difficult to direct thebutton to a desired location. However, the second and third filaments790, 791 can assist in manipulating the button 710 to a desired locationin which the flat bottom surface 720 rests on the femoral cortex andfaces the femoral tunnel 1004, as shown in FIG. 16F. This allows thecoils 760 a, 760 b and graft 802 associated therewith to be disposed inthe bone tunnel 1002 and the knot 752 to be located outside of butadjacent to the bone tunnel 1002.

A variety of techniques can be used to flip or reorient the button, butin the illustrated embodiment, shown in FIG. 16F, a force in anapproximate direction K is applied to the graft 802, thus tensioning thegraft and causing the button 710 to flip. In other embodiments, asurgeon can selectively apply tension to the graft 802 and the secondand third filaments 790, 791 to flip the button 710 to its desiredlocation. Once the surgeon has oriented the button 710 as desired, thesurgeon can confirm its location as lying flat on the femoral cortex,directly adjacent to the femoral tunnel 1004, using a variety oftechniques, including by using tactile feedback received from pullingthe second and third filaments 790, 791 and the graft 802, and/or usingvisual aids.

Once the body 710 is disposed at its desired location, tension can beapplied to the terminal ends 754 t, 755 t of the limbs 754, 755 toadjust the circumference of the coils 760 a, 760 b, thereby moving thegraft 802 within the bone tunnel 1002 to a desired location. Thecircumferences of the coils 760 a, 760 b can be adjusted using a numberof different techniques, including those described herein. In oneexemplary embodiment, illustrated in FIG. 16G, the first and secondterminal ends 754 t, 755 t can be selectively pulled in an approximatedirection N to advance the graft 802 through the tunnel 1002.

Once the implant 800 and graft 802 are positioned in their desiredlocations, excess filaments can be removed, including portions of theterminal ends 754 t, 755 t and the second and third filaments 790, 791.In some embodiments the second and third filaments can be completelyremoved, while care can be taken to ensure that enough material remainswith respect to the terminal ends 754 t, 755 t so as not to negativelyimpact the integrity of the knot 752. Then the remaining portions of therepair can be carried out, such as steps related to tibial fixation

FIG. 16H illustrates an embodiment of an ACL repair method in which afilament 750′ is used to form four coils 760 a′, 760 b′, 760 c′, 760 d′,two (760 a′, 760 c′) of which are associated with a first graft 802′ andtwo (760 b′, 760 d′) of which are associated with a second graft 804′.As shown in FIG. 16H, the cortical button 710′ is already oriented orflipped so that the top surface 720′ rests on the femoral cortex andfaces the femoral tunnel 1004, for instance relying on techniquesdisclosed herein, and thus circumferences of the coils 760 a′, 760 b′,760 c′, 760 d′ can be adjusted to selectively locate them within thebone tunnel 1002. These techniques include, for instance, thosediscussed above with respect to FIGS. 6A and 6B. In one exemplaryembodiment, tension can be alternately applied in an approximatedirection P to first and second terminal ends 754 t′, 755 t′ to advancethe grafts 802′, 804′ in increments of approximately 1 centimeter.Alternatively, the grafts 802′, 804′ can be advanced by using aconfiguration in which the first and second terminal ends 754 t′, 755 t′are tied together and held in one hand while tension in the approximatedirection Q is applied to the grafts 802′, 804′ by another hand. Thesurgeon can then alternate between pronation and supination to tightenthe filament limbs, and thereby the coils 760 a′, 760 b′, 760 c′, 760d′, which in turn advances the grafts 802′, 804′ proximally through thebone tunnel 1002.

The grafts 802′, 804′ can be advanced to a desired location, for exampleup to the passing channel 1007 of the femoral tunnel 1004. When a graft802′, 804′ reaches the passing channel 1007, typically the resistance totightening of the coils 760 a′, 760 b′, 760 c′, 760 d′ noticeablyincreases. In some embodiments, such as that illustrated in FIG. 16H,one or more loops 760 a′, 760 c′ can have a smaller circumference thanother loops 760 b′, 760 d′ so that one graft 802′ is more proximallylocated than the other graft 804′. As also illustrated in FIG. 16H, anyshuttle filaments used in the method can be removed, and the terminalends 754 t′, 755 t′ can be shortened as described herein.

A person skilled in the art will also recognize how other embodimentsdescribed herein or derivable therefrom can be easily adapted for usewith the procedures described herein, and in some instances can provideadditional benefits. By way of non-limiting example, for embodimentssuch as those illustrated in FIGS. 14A, 14B, and 16C in which a singlefilament is used for purposes of shuttling the body, removal of thefilament after placement of the cortical button can be easier than ifseparate filaments are tied to respective leading and trailing ends ofthe button.

The ability to control two independently tensioned ligament grafts in asingle tunnel using a single cortical button is an improvement overexisting techniques for ACL repairs. In existing methods for performingACL repairs, a cortical button having filament associated therewith canonly control a single bundle of ligament graft. Thus, if independentmovement of multiple ligaments is needed, each ligament is typicallyassociated with its own cortical button. Some surgeons use adouble-tunnel technique to implant two ligaments, thus fixing each graftbundle in separate tunnels. Double-tunnel techniques likewise requireone button per bundle. Thus, the methods described and resulting fromdisclosures herein represent improved ACL repair techniques because theyallow for two ligament bundles to be independently moved using a singlebutton, and doing so in a single tunnel. This results in procedures thathave a reduced risk of complications and is generally less complex thanexisting procedures. A person skilled in the art will recognize that thedisclosures pertaining to independently controlling two filament loopscan be broadly applied to a variety of implant designs and surgicalprocedures, and can even be applied to non-medical fields withoutdeparting from the spirit of the present disclosure.

One skilled in the art will appreciate further features and advantagesof the invention based on the above-described embodiments. Accordingly,the invention is not to be limited by what has been particularly shownand described, except as indicated by the appended claims. By way ofnon-limiting example, the exemplary ACL repair methods described hereinwith respect to FIGS. 16A-16H can be adapted for use with the otherimplant configurations described herein or derivable from thedisclosures herein. All publications and references cited herein areexpressly incorporated herein by reference in their entirety.

What is claimed is:
 1. A surgical implant, comprising: a body having aplurality of thru-holes formed therein; and a filament having: anoverhand knot located on a top side of the body, the overhand knothaving a first collapsible opening, a second collapsible opening, and athird collapsible opening; first, second, third, and fourth filamentloops extending from the overhand knot towards the body, each filamentloop passing through two thru-holes of the plurality of thru-holes, andeach filament loop having a distal end disposed on a bottom side of thebody; and at least two tensioning limbs extending from the overhandknot, in a direction opposite to a direction that the filament loopsextend from the overhand knot, wherein a portion of filament of thefirst filament loop disposed on the top side of the body extends throughthe first collapsible opening, a portion of filament of the secondfilament loop disposed on the top side of the body extends through thesecond collapsible opening, a portion of filament of the third filamentloop disposed on the top side of the body extends through the firstcollapsible opening, and a portion of filament of the fourth filamentloop disposed on the top side of the body extends through the thirdcollapsible opening, with the first, second, and third collapsibleopenings being collapsible around, and thus engageable with, therespective filament portion extending therethrough to form the overhandknot.
 2. The surgical implant of claim 1, wherein the plurality ofthru-holes comprises two outer thru-holes and two inner thru-holes, eachouter thru-hole being located adjacent to respective opposed terminalends of the body and the inner thru-holes being disposed between theouter thru-holes, and wherein the first and third filament loops aredisposed in each of the outer thru-holes and the second and fourthfilament loops are disposed in each of the inner thru-holes.
 3. Thesurgical implant of claim 1, wherein the plurality of thru-holescomprises two outer thru-holes and two inner thru-holes, each outerthru-hole being located adjacent to respective opposed terminal ends ofthe body and the inner thru-holes being disposed between the outerthru-holes, and wherein the first, second, third, and fourth filamentloops are each disposed in each of the inner thru-holes.
 4. The surgicalimplant of claim 1, wherein at least one of the at least two tensioninglimbs is configured to adjust a circumference of at least one of thefirst, second, third, and fourth filament loops when tension is appliedthereto.
 5. The surgical implant of claim 1, wherein the firstcollapsible opening has a central location such that the secondcollapsible opening is located on one side of the first collapsibleopening and the third collapsible opening is located on a second,approximately opposite side of the first collapsible opening.
 6. Thesurgical implant of claim 1, wherein the first, second, third, andfourth filament loops are configured to hold a combined average maximumload of at least about 765 N.
 7. A surgical implant, comprising: a bodyhaving a plurality of thru-holes formed therein; and a suture filamentextending through the body and configured to form: an overhand knothaving a first collapsible opening, a second collapsible opening, and athird collapsible opening, the overhand knot being located on a top sideof the body; a first coil formed as a result of a first suture limbextending from the overhand knot extending through a through hole of theplurality of thru-holes formed in the body to a bottom side of the body,then through another through hole of the plurality of thru-holes formedin the body, and then through the first collapsible opening of theoverhand knot; a second coil formed as a result of a second suture limbextending from the overhand knot extending through a through hole of theplurality of thru-holes formed in the body to the bottom side of thebody, then through another through hole of the plurality of thru-holesformed in the body, and then through one of the first, second, and thirdcollapsible openings of the overhand knot; a third coil formed as aresult of the first suture limb extending from passing through the firstcollapsible opening through a through hole of the plurality ofthru-holes formed in the body to the bottom side of the body, thenthrough another through hole of the plurality of thru-holes formed inthe body, and then through the second collapsible opening of theoverhand knot, with a portion of the first suture limb extending throughthe second collapsible opening forming a first tensioning limb; and afourth coil formed as a result of the second suture limb extending frompassing through one of the first, second, and third collapsible openingsthrough a through hole of the plurality of thru-holes formed in the bodyto the bottom side of the body, then through another through hole of theplurality of thru-holes formed in the body, and then through either thethird opening of the overhand knot if the second suture limb did notpreviously extend through the third opening, or one of the first andsecond collapsible openings of the overhand knot if the second suturelimb did extend through the third opening, with a portion of the secondsuture limb extending through either the third opening of the overhandknot if the second suture limb did not previously extend through thethird opening, or one of the first and second collapsible openings ofthe overhand knot if the second suture limb did extend through the thirdopening, forming a second tensioning limb; wherein the first, second,and third collapsible openings are collapsed around, and thus engagedwith, the respective first and second suture limbs extendingtherethrough to form the overhand knot.
 8. The surgical implant of claim7, wherein the plurality of thru-holes comprises two outer thru-holesand two inner thru-holes, each outer thru-hole being located adjacent torespective opposed terminal ends of the body and the inner thru-holesbeing disposed between the outer thru-holes, and wherein the first andthird coils are disposed in each of the outer thru-holes and the secondand fourth coils are disposed in each of the inner thru-holes.
 9. Thesurgical implant of claim 7, wherein the plurality of thru-holescomprises two outer thru-holes and two inner thru-holes, each outerthru-hole being located adjacent to respective opposed terminal ends ofthe body and the inner thru-holes being disposed between the outerthru-holes, and wherein the first, second, third, and fourth coils areeach disposed in each of the inner thru-holes.
 10. The surgical implantof claim 7, wherein at least one of the first and second tensioninglimbs is configured to adjust a circumference of at least one of therespective first and third coils and second and fourth coils whentension is applied thereto.
 11. The surgical implant of claim 7, whereinthe first collapsible opening has a central location such that thesecond collapsible opening is located on one side of the firstcollapsible opening and the third collapsible opening is located on asecond, approximately opposite side of the first collapsible opening.12. The surgical implant of claim 7, wherein the first, second, third,and fourth coils are configured to hold a combined average maximum loadof at least about 765 N.